Product Details

SNP ID

rs144341542

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:22120167 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCCACCTGCGCCGTGTGGAAGCC[A/G]CGGCCACAGCACAGCAGCTCACAGC

Phenotype

MIM: 603490

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WNT4 PubMed Links

Gene Details

Gene

WNT4

Gene Name

Wnt family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030761.4	1112	Silent Mutation	CGC,CGT	R313R	NP_110388.2
XM_011541597.2	1112	Silent Mutation	CGC,CGT	R335R	XP_011539899.1
XM_011541598.2	1112	Silent Mutation	CGC,CGT	R258R	XP_011539900.1
XM_011541599.1	1112	Intron			XP_011539901.1

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